Avian E. coli vaccine for protection against colibacillosis

ABSTRACT

A genetic deletion mutant live  E. coli  vaccine suitable for mass application to poultry, including chickens, is provided. Also provided is a safe and effective method to protect poultry against the ravages of  Escherichia coli  bacillosis infection and disease in which a live mutant aroA-gene deleted  E. coli  immunogen is administered to chickens, turkeys and the like via mass application routes such as coarse sprays and drinking water.

This application is a continuation of US Application Ser. No. 10/837,793, filed May 3, 2004, now U.S. Pat. No. 7,357,935, which claims priority from provisional Application Ser. No. 60/470,471, filed May 14, 2003. The entire disclosure of these applications is hereby incorporated by reference.

FIELD OF THE INVENTION

The present invention relates to avian vaccines against E. coli infection. In particular, the invention is directed to mutant strain E. coli vaccines which are useful for poultry, and especially chickens. The invention also relates to a novel aroA gene-deleted E. coli microorganism immunogen which is useful and effective in a vaccine via spray or drinking water against E. coli-induced colibacillosis, a devastating poultry illness.

BACKGROUND OF THE INVENTION

Colibacillosis is a common systemic disease of economic importance in poultry and occurs worldwide. This Escherichia coli (E. coli) infection occurs as an acute fatal septicemia or subacute pericarditis and airsacculitis, as well as perihepatitis, arthritis, and also cellulitis. Among bacterial infections, colibacillosis is very often the first cause of morbidity and mortality in poultry. Large numbers of E. coli are maintained in the poultry house environment through fecal contamination. Systemic infection occurs when large numbers of pathogenic E. coli gain access to the bloodstream via the respiratory tract or intestine. Bacteremia progresses to septicemia and death, or the infection extends to serosal surfaces, pericardium, joints and other organs.

The literature suggests that serotypes O1, O2 and O 78 of E. coli associated with colibacillosis are the most common serotypes found in chickens and turkeys. Many isolated strains are also untypeable and are considered especially virulent.

Treatment strategies include control of predisposing infections or environmental factors, and early use of antibiotics. Unfortunately, a high frequency of resistance to tetracycline, kanamycin, neomycin, cephalotin, streptomycin and erythromycin has been observed. Many strains are also resistant to several antibiotics. Wide spread sensitivity to ampicillin and chloramphenicol has also been observed.

Although there is a commercial live E. coli vaccine available for use against colibacillosis associated with infection by E. coli O 78 in turkeys, there appears to be no fully safe and effective E. coli vaccines for use in chickens. In particular, there does not appear to be any live, attenuated, mutant aroA gene-deleted E. coli vaccine for poultry commercially available. There also does not appear to be an especially efficacious E. coli vaccine that is suitable for mass administration via aerosol spray or drinking water, for example.

Therefore, it is an object of this invention to provide a safe and effective live E. coli vaccine, suitable for use in chickens.

It is another object of this invention to provide a method for the prevention or amelioration of colibacillosis in poultry which is safe and effective when used in chickens.

It is a feature of this invention that the E. coli vaccine is suitable for mass application.

It is an advantage of this invention that the live vaccine provides both a good cellular and a good humoral immunity response in the host.

SUMMARY OF THE INVENTION

The present invention provides the gene deleted Escherichia coli mutant, E. coli aroA-microorganism having the identifying characteristics of the strain which was deposited with the American Type Culture Collection and assigned number PTA-5094.

The present invention also provides an avian vaccine composition which comprises an immunogenically effective amount of said E. coli aroA-microorganism and a pharmacologically acceptable carrier.

The present invention further provides a method for the prevention or amelioration of colibacillosis in poultry which comprises administering to said poultry an immunogenically effective amount of said E. coli aroA-microorganism.

Further provided as part of the invention is a vaccine for chickens and other poultry against colibacillosis which comprises an immunogenically effective amount of an E. coli aroA-deletion mutant in a pharmacologically acceptable carrier.

Other features of the invention will be come more apparent from the detailed description set forth hereinbelow.

DETAILED DESCRIPTION OF THE INVENTION

Avian colibacillosis in domestic poultry is frequently associated with Escherichia coli (E. coli) serotype O78. Infection commonly occurs via the respiratory tract, often following exposure to, or infection by, other poultry community diseases such as mycoplasmosis, infectious bronchitis, Newcastle's disease, hemorrhagic enteritis or turkey bordetellosis. In chickens, colibacillosis generally affects broilers between 3 to 10 weeks of age and is associated with high morbidity and mortality. The most severe manifestation of avian colibacillosis is septicemia which is characterized by pericarditis, perihepatitis and airsacculitis. Cellulitis is also a formidable problem. Isolates of E. coli from poultry are frequently resistant to drugs such as ampicillin, chloramphenicol, oxytetracycline, neomycin, gentamicin, nitrofurans, nalidixic acid, polymixin B, sulfonamides, or the like. Moreover, at present, there appears to be no commercially available E. coli vaccines for chickens.

Surprisingly, it has now been found that the E. coli aroA deletion mutant, E. coli aroA-deposited with the American Type Culture Collection (ATCC) at 10801 University Boulevard, Manassas, Va. 20110 USA on Mar. 27, 2003 and having ATCC accession number PTA-5094 is safe and effective for use against avian colibacillosis in chickens. Advantageously, the E. coli aroA-PTA-5094 of the invention, when administered to chickens, provides good cellular and humoral immune responses and said E. coli aroA-PTA-5094 may be easily produced and may be administered via mass application, e.g. coarse spray or drinking water.

As used in the specification and claims, the term E. coli aroA-PTA-5094 designates the Escherichia coli aroA deletion mutant microorganism which was deposited with the ATCC on Mar. 27, 2003 and was assigned ATCC number PTA-5094. This term is also intended to encompass other strains of E. coli aroA-gene-deletion mutants which are prepared in substantially the same manner as set forth herein, and which have substantially the same immunogenic characteristics thereof.

The E. coli aroA gene deleted mutant strain of the invention may be further serially passaged using media and techniques available to the skilled artisan. Serial passaging can serve to further attenuate the strain to make it more suitable as a vaccine immunogen. Up to about 10 serial passages are contemplated herein, with about 3 to 5 being preferred.

The E. coli aroA deletion mutant of the invention has the distinct advantage that the surface appendages such as type 1 fimbriae and flagella, which have been shown to be important in the pathogenesis of avian colibacillosis, are still expressed. (LaRagione, R. M.; Sayus, A. R.; and Woodward, M. J., Epidemiology and Infection, 2000, 124:351-363 and LaRagione, R. M.; Cooly, W. A.; and Woodward, M. J., Journal of Medical Microbiology, 2000, 49:327-338). Fully defined genetic deletion vaccines are preferable as candidates for live vaccines, offering the potential of combined safety and a high degree of efficacy in the host. Particularly desirable are deletion mutants that cannot revert to a wild-type phenotype. In actual practice, a defined E. coli aroA-mutant deficient for the biosynthesis of aromatic amino acids was constructed in a pathogenic E. coli strain to produce the E. coli aroA-PTA-5094 of the invention. Said E. coli aroA-PTA-5094 is safe and efficacious in chicks against a wild-type E. coli challenge. Accordingly, the present invention also provides a method for the prevention or amelioration of avian colibacillosis in poultry which comprises administering to said poultry an immunogenically effective amount of E. coli aroA-PTA-5094.

Immunogenically effective amounts may vary according to the age and size of the host, the severity of the infection, the virility of the pathogen, the mode of administration or the like. In general, suitable effective amounts per dosage unit may be about 10² to 10¹⁴ colony forming units (cfu), preferably about 5.0×10² to 5.0×10¹⁰ cfu, more preferably about 3.0×10⁶ cfu to 6.0×10⁶ cfu, and even more preferably about 5.0×10⁶ cfu to 6.0×10⁶ cfu. One or two dosage units may be contemplated by the skilled artisan. If two dosage units are selected, then vaccination at about day 1 post-hatch and again at about one week to two weeks of age is preferred. A dosage unit is desirably about 0.5 to 1 mL of vaccine per bird, but that quantity may be optimized to deliver an immunogenically effective amount of the microorganism immunogen hereinabove described.

Poultry suitable for use in the method of invention include chickens, ducks, turkeys, geese, bantams, quail, pheasant, pigeons, or the like, preferably commercially important poultry such as chickens, ducks, geese and turkeys, more preferably chickens and turkeys, particularly preferably chickens.

The E. coli aroA-PTA-5094 of the invention may be administered by any conventional means, preferably an economically viable means for the poultry industry such as mass administration via spray or drinking water. It is quite unexpected that E. coli, a natural pathogen of the respiratory mucosa, can be applied via a spray (preferably aerosol) route, and still be safe as well as efficacious. It would normally be expected that a vaccine against such a potently lethal pathogen, especially bacteria, should only be provided via injection or some other route. The aroA-mutation strain of the invention is safe for spray administration. In actual practice, the E. coli aroA-PTA-5094 is admixed with a liquid carrier and administered as a spray or as a drinking water additive. Accordingly, the present invention further provides an avian vaccine composition which comprises an immunogenically effective amount of E. coli aroA-PTA-5094 and a pharmacologically acceptable carrier.

Pharmacologically acceptable carriers suitable for use in the vaccine composition of the invention may be any conventional liquid carrier suitable for veterinary pharmaceutical compositions, preferably a balanced salt solution suitable for tissue or cell culture media such as sterile phosphate buffered saline, more preferably distilled water. Other suitable media can include emulsions. The vaccine of the invention may also be adjuvanted by the skilled technician. When application of the vaccine is via drinking water, non-fat dry milk may be utilized as a carrier. The non-fat dry milk appears to stabilize the vaccine, and perhaps neutralizes the action of some trace minerals that can affect viability.

In addition to the E. coli aroA-PTA-5094 microorganism as active ingredient, it is contemplated the vaccine composition of the invention may also contain other active components such as an avian immunogenic antipathogenic compound directed against avian leukosis, reticuloendotheliosis, infectious bronchitis, infectious bursal disease, Newcastle disease, avian adenovirus disease, avian reovirus disease, fowl pox disease, infectious laryngotracheitis, avian influenza, infectious coryza, fowl typhoid, coccidiosis, cryptosporidiosis, fowl cholera, or the like.

In one embodiment of the invention, the E. coli aroA-PTA-5094 microorganism of the invention may be incorporated into liposomes using known technology such as that described in Nature, 1974, 252:252-254 or Journal of Immunology, 1978, 120:1109-1113. In another embodiment of the invention, the E. coli aroA-PTA-5094 microorganism of the invention may be conjugated to suitable biological compounds such as polysaccharides, peptides, proteins, or the like, or a combination thereof using protocol available to the skilled artisan.

The vaccine of the invention according to the embodiments herein described is to be considered efficacious against all serotypes of E. coli colibacillosis, including serotypes O1, O2 and O78, as well as the especially virulent untyped serotypes. The vaccine herein described is efficacious against septicemia, pericarditis, airsacculitis, periphepatitis, arthritis, and particularly cellulitis. The latter is often associated with colibacillosis, but can be a significant problem in itself.

For a more clear understanding of the invention, the following examples are set forth below. These examples are merely illustrative and are not understood to limit the scope or underlying principles of the invention in any way. Indeed, various modifications of the invention, in addition to those shown and described herein, will become apparent to those skilled in the art from the examples set forth hereinbelow and the foregoing description. Such modifications are also intended to fall within the scope of the appended claims.

EXAMPLE 1 Construction of aroA Gene Deleted E. coli Mutant

I) Recipient

The parental organism is an avian isolate of E. coli isolated from a clinical case of avian colibacillosis submitted to the Veterinary Laboratories Agency (VLA), Addlestone, Surrey, UK and serotyped at VLA in 1995. The parent strain was selected for its colonization, invasion, persistence and pathogenicity in one-day-old SPF chicks and by in vitro characterization for its antibiotic sensitivity pattern. The recipient strain was generated by conjugation between the transformed donor (E. coli K12 S17 λ pir harboring PNG101 with aroA harboring 100 bp deletion) and wild-type parent strain (wild-type E. coli isolate EC34195).

II) Characterization of the Deletion

The aroA gene, which encodes 3-phosphoenolpyruvylshikimate-5-phosphate synthetase, an enzyme of the common aromatic biosynthetic pathway, is located adjacent and promoterdistal to serC in the serC-aroA operon. Loss of function for the aroA gene in the recipient results in a requirement for aromatic metabolites, including tyrosine, phenylalanine, tryptophan, p-aminobenzoate (PABA) and 2,3-dihydroxybenzoate. The requirement for PABA, a metabolite not found in vertebrate tissues, results in attenuation of in vivo growth.

III) Construction of the aroA Deleted E. coli Mutant

a) PCR primers are designed incorporating SrfI and BglII restriction sites and stop codons to amplify two separate PCR products of approximately 650 bp for the 5′ and 3′ ends of the aroA gene from the poultry E. coli O78 isolate described above.

b) Both PCR products are digested with BglII for 2 hours, electrophoresis is run for 1 hour at 100 volts, the bands are excised and the respective bands are purified using SephaGlas bandprep kit.

c) Equal volumes of each purified PCR product are mixed and ligated into pCR2.1.

d) Ligated plasmid harboring aroA are transformed into DH5α maxi-competent cells and cloning is confirmed by restriction enzyme mapping and PCR.

e) Complete aroA gene with deletion from pCR2.1 is excised with EcorV and SpeI then purified and ligated into a predigested (SpeI) suicide vector (SacB, pKNG101), transformed into competent E. coli K12 S17 λ pir and cloning is confirmed by restriction enzyme mapping and PCR.

f) A conjugation is performed between donor (E. coli S17 λ pir harboring pKNG101 with aroA harboring 100 bp deletion) and wild-type E. coli isolate.

g) Colonies appearing after 48 hours incubation at 37° C. are subcultured onto minimal media supplemented with gentamicin and streptomycin and aromatic amino acids (20 mg/l of each of DL tryptophan, DL phenylalanine and DL tyrosine). Individual colonies are tested by PCR. Colonies that yielded a wild-type PCR product and mutated PCR product of some 100 bp smaller are retained for further studies.

h) Single crossovers are cultured in LB-G broth supplemented with 10% sucrose at 37° C. with gentle agitation for 16 hours. Serial dilutions of the overnight cultures are plated onto LB-G plates supplemented with 10% sucrose and incubated at 37° C. for 16 hours.

i) Colonies which grow on the 10% sucrose LB-G plates are subcultured onto each of LB-G, LB-G+gentamicin and streptomycin and minimal and incubated at 37° C. for 16 hours. Colonies only growing on the LB-G plates (double crossovers) are subcultured onto 5% sheep's blood agar and maintained at 4° C.

IV) Intermediate Cloning Vector

Suicide vector (SacB, PNG101) was the intermediate cloning vector. Conjugation was performed between donor (S17 harboring PNG101 with aroA harboring 100 bp deletion) and wild-type E. coli isolate.

EXAMPLE 2 Preparation of Master Seed

The E. coli aroA-strain (constructed in Example 1) is grown on tryptic soy agar plate once and passed 3 times in tryptic soy broth. The culture is distributed into glass vials, sealed and lyophilized.

EXAMPLE 3 Evaluation of the Efficacy of E. coli aroA-Live in Chickens Against Avian Colibacillosis After one Vaccination

In this evaluation, 96 SPF white leghorn chickens are divided into 3 groups of 32 each. Birds are hand picked and placed in an arbitrarily assigned isolater. Each test group is housed in 2 isolaters containing 16 birds each.

Group A is vaccinated at 1 day old by coarse spray using a hand-held sprayer. At one day of age, birds in test group A are grouped together in a small container and the vaccine is sprayed to the heads of the birds until the calibrated dosage has been given. The E. coli aroA-microorganism of Example 2 is diluted with sterile phosphate buffered saline (PBS) to a titer of 5.0×10⁶ cfu per dose (1 mL per bird).

At 6 weeks of age, Group A and Group B (unvaccinated) are challenged intratracheally (IT) with a 1.0 mL dose of 1.0×10⁹ cfu E. coli O78.

Test Group C is unvaccinated and unchallenged (negative control group). Vaccinates and control birds are reared in separate isolaters until the completion of the study.

All birds are under veterinary care with feed and water available ad libitum. Birds are observed daily for 7 days post-challenge. At the end of the 7-day post-challenge period, all surviving birds are necropsied and examined for the presence of lesions typical of colibacillosis. Non-surviving birds and birds that demonstrated any of the grossly visible lesions such as perihepatitis, pericarditis, airsacculitis, cellulitis, or arthritis are considered positive for colibacillosis.

The results are shown in Table I.

TABLE I % Surviving birds with gross % Positive Test Vaccination Challenge % lesions for Group Route Route Mortality Hep^(b) Card^(c) Air^(d) Cell^(e) Arth^(f) Colibacillosis A Coarse IT 3.1^(a) 22.6 6.5 16.13 3.2 0 29.0 spray B None IT 28.1 91.3 82.6 86.9 47.8 17.4 96.9 C None None 0 0 0 0 0 0 0 ^(a)One bird died at one day post-vaccination. The cause could not be determined but was likely nonspecific early chick mortality often related to yolk sac or navel infection. ^(b)Perihepatitis ^(c)Pericarditis ^(d)Airsacculitis ^(e)Cellulitis ^(f)Arthritis

As can be seen from the data in Table I, the E. coli aroA-vaccine of the invention is safe and efficacious for the prevention of colibacillosis in chickens caused by E. coli O78, when said vaccine is administered at one day of age.

EXAMPLE 4 Evaluation of the Efficacy of E. coli aroA-Live Vaccine in Chickens Against Avian Colibacillosis After Two Vaccinations

In this evaluation, 96 SPF white leghorn chickens are divided into 3 groups of 32 each. Birds are hand picked and placed in an arbitrarily assigned isolater. Each test group is housed in 2 isolaters, each containing 16 birds.

Group A (vaccinates) are vaccinated at one day of age by coarse spray, as described in Example B and again at 1 week of age by the drinking water route. At one week of age, birds are deprived of drinking water for 3 h. The E. coli aroA-vaccine of Example 2 is diluted and mixed with a measured quantity of cool distilled water to a final titer of 5.0×10⁶ cfu. The measured quantity of distilled water is that amount previously determined to be consumed in one hour.

At 6 weeks of age, Group A (vaccinated) and Group B (unvaccinated) are challenged intratracheally (IT) with a 1.0 mL dose of 1.0×10⁹ cfu E. coli O78.

Test Group C is unvaccinated and unchallenged (negative control group). Vaccinates and control birds are reared in separate isolaters until the completion of the study.

All birds are under veterinary care with feed and water available ad libitum. Birds are observed daily for 7 days post-challenge. At the end of the 7-day post-challenge period, all surviving birds are necropsied and examined for the presence of lesions typical of colibacillosis. Non-surviving birds and birds that demonstrated any of the grossly visible lesions such as perihepatitis, pericarditis, airsacculitis, cellulitis, or arthritis are considered positive for colibacillosis.

The results are shown in Table II.

TABLE II % Surviving birds with gross % Positive Test Vaccination Challenge % lesions for Group Route Route Mortality Hep^(b) Card^(c) Air^(d) Cell^(e) Arth^(f) Colibacillosis A Coarse IT 6.3^(a) 10 23.3 20 0 0 36.7 Spray/Drinking Water B None IT 28.1 91.3 82.6 86.9 47.8 17.4 96.9 C None None 0 0 0 0 0 0 0 ^(a)Two birds died at 2 days post-vaccination via the coarse spray route. The cause could not be determined but was likely nonspecific early chick mortality often related to yolk sac or navel infection. ^(b)Perihepatitis ^(c)Pericarditis ^(d)Airsacculitis ^(e)Cellulitis ^(f)Arthritis

As can be seen from the data in Table II, the E. coli aroA-vaccine of the invention is safe and efficacious for the prevention of colibacillosis in chickens caused by E. coli O78, when said vaccine is administered at one day of age via coarse spray and again at one week of age via drinking water.

EXAMPLE 5 Further Evaluation of the Efficacy of E. coli aroA-Live Vaccine in Chickens Against Avian Colibacillosis (Serotype O78) After Two Vaccinations

This study investigated the efficacy of an E. coli aroA-live vaccine in preventing colibacillosis in chickens following intratracheal challenge with a virulent strain of E. coli—serotype O78. Each bird in test group #1 (32 birds) was vaccinated by coarse spray at 1 day of age and again in the drinking water at 1 week of age with one bird dose of E. coli aroA-vaccine. Birds in test group #2 (32 birds) served as unvaccinated challenged controls. Birds in test group #3 (32 birds) were not vaccinated and were not challenged. All the birds in groups #1 and #2 were challenged intratracheally at 6 weeks of age with 1.5×10⁹ cfu per dose of E. coli O78. At 7 days post challenge, all surviving birds were necropsied and examined for the presence of grossly visible lesions typical of colibacillosis (perihepatitis, pericarditis, airsacculitis, cellulitis, or arthritis).

There were no unfavorable reactions (death or other clinical signs) that were attributable to the administration of FDAH E. coli aroA-live vaccine, an indication of its safety for mass administration.

The virulent strain of E. coli O78 caused 28.1% mortality (9 out of 32 birds died) in the unvaccinated challenged controls (group #2) during the 7-day post-challenge period. The mortality caused by virulent strain of E. coli O78 in FDAH E. coli aroA-live vaccine vaccinated birds was 0% (0 out of 32 birds died) during the 7-day post-challenge period.

The rates of colibacillosis were statistically analyzed between vaccinated challenged birds and unvaccinated challenged control birds. There was a significant difference (p<0.0001) between the vaccinated and unvaccinated challenged birds with gross lesions typical of colibacillosis. The prevented fraction was 72.4% (95% Cl 53.7, 83.6).

Based on the present study, it was concluded that FDAH E. coli aroA-live vaccine with a titer of 3.2×10⁶ cfu per dose was safe and efficacious for the prevention of colibacillosis in chickens caused by E. coli O78 when it was administered at one day of age by coarse spray and again at 1 week of age in the drinking water.

EXAMPLE 6 Further Evaluation of the Efficacy of E. coli aroA-Live Vaccine in Chickens Against Avian Colibacillosis (Serotype O78) After One Vaccination

This study investigated the efficacy of an E. coli aroA-live vaccine in preventing colibacillosis in chickens following intratracheal challenge with a virulent strain of E. coli O78. Each bird in test group #1 (32 birds) was vaccinated by coarse spray at 1 day of age with one bird dose of E. coli aroA-vaccine. Birds in test group #2 (32 birds) served as unvaccinated challenged controls. Birds in test group #3 (32 birds) were not vaccinated and were not challenged. All the birds in groups #1 and #2 were challenged intratracheally at 6 weeks of age with 1.5×10⁹ cfu per dose of E. coli O78. At 7 days post challenge, all surviving birds were necropsied and examined for the presence of grossly visible lesions typical of colibacillosis (perihepatitis, pericarditis, airsacculitis, cellulitis, or arthritis).

There were no unfavorable reactions (death or other clinical signs) that were attributable to the administration of FDAH E. coli aroA-live vaccine, an indication of its safety for mass administration.

The virulent strain of E. coli O78 caused 28.1% mortality (9 out of 32 birds died) in the unvaccinated challenged controls during the 7-day post-challenge period. The mortality caused by virulent strain of E. coli O78 in FDAH E. coli aroA-live vaccine vaccinated birds was 0% (0 out of 32 birds died) during the 7-day post-challenge period.

The rates of colibacillosis were statistically analyzed between vaccinated challenged birds and unvaccinated challenged control birds. There was a significant difference (p<0.0001) between the vaccinated and unvaccinated challenged birds with gross lesions typical of colibacillosis. The prevented fraction was 76.5% (95% Cl 57.9, 86.9).

Based on the present study, it was concluded that FDAH E. coli aroA-live vaccine containing 3.2×10⁶ cfu per dose was safe and efficacious for the prevention of colibacillosis in chickens caused by E. coli O78 when it was administered at one day of age by coarse spray.

EXAMPLE 7 Evaluation of the Efficacy of E. coli aroA-Live Vaccine in Chickens Against Avian Colibacillosis (Virulent Untyped Serotype) After Two Vaccinations

This study investigated the efficacy of an E. coli aroA-live vaccine in preventing colibacillosis in chickens following intratracheal challenge with a virulent E. coli which is untyped. Each bird in test group #1 (32 birds) was vaccinated by coarse spray at 1 day of age and again in the drinking water at 1 week of age with one bird dose of E. coli aroA-vaccine. Birds in test group #2 (32 birds) served as unvaccinated challenged controls. Birds in test group #3 (32 birds) were not vaccinated and were not challenged. All the birds in groups #1 and #2 were challenged intratracheally at 6 weeks of age with 2.5×10¹⁰ cfu per dose of virulent E. coli. At 7 days post challenge, all surviving birds were necropsied and examined for the presence of grossly visible lesions typical of colibacillosis (perihepatitis, pericarditis, airsacculitis, cellulitis, or arthritis).

There were no unfavorable reactions (death or other clinical signs) that were attributable to the administration of FDAH E. coli aroA-live vaccine, an indication of its safety for mass administration.

The virulent E. coli did not cause mortality in the unvaccinated challenged controls or the FDAH E. coli aroA-live vaccine vaccinated birds during the 7-day post-challenge period.

The rates of colibacillosis were statistically analyzed between vaccinated challenged birds and unvaccinated challenged control birds. There was a significant difference (p<0.0001) between the vaccinated and unvaccinated challenged birds with gross lesions typical of colibacillosis. The prevented fraction was 87.1% (95% Cl 61.9, 95.6).

Based on the present study, it was concluded that FDAH E. coli aroA-live vaccine with a titer of 3.2×10⁶ cfu per dose was safe and efficacious for the prevention of colibacillosis in chickens caused by virulent E. coli when it was administered at one day of age by coarse spray and again at 1 week of age in the drinking water.

EXAMPLE 8 Evaluation of the Efficacy of E. coli aroA-Live Vaccine in Chickens Against Avian Colibacillosis (Virulent Untyped Serotype) After One Vaccination

This study investigated the efficacy of an E. coli aroA-live vaccine in preventing colibacillosis in chickens following intratracheal challenge with a virulent E. coli which is untyped. Each bird in test group #1 (32 birds) was vaccinated by coarse spray at 1 day of age with one bird dose of E. coli aroA-vaccine. Birds in test group #2 (32 birds) served as unvaccinated challenged controls. Birds in test group #3 were unvaccinated and were not challenged. All the birds in groups #1 and #2 were challenged intratracheally at 6 weeks of age with 2.5×10¹⁰ cfu per dose of virulent E. coli. At 7 days post challenge, all surviving birds were necropsied and examined for the presence of grossly visible lesions typical of colibacillosis (perihepatitis, pericarditis, airsacculitis, cellulitis, or arthritis).

There were no unfavorable reactions (death or other clinical signs) that were attributable to the administration of FDAH E. coli aroA-live vaccine, an indication of its safety for mass administration.

The virulent E. coli did not cause mortality in the unvaccinated challenged controls or the FDAH E. coli aroA-live vaccine vaccinated birds during the 7-day post-challenge period.

The rates of colibacillosis were statistically analyzed between vaccinated challenged birds and unvaccinated challenged control birds. There was a significant difference (p<0.0001) between the vaccinated and unvaccinated challenged birds with gross lesions typical of colibacillosis. The prevented fraction was 66.6% (95% Cl 39.8, 81.5).

Based on the present study, it was concluded that FDAH E. coli aroA-live vaccine with a titer of 3.2×10⁶ cfu per dose was safe and efficacious for the prevention of colibacillosis in chickens caused by virulent E. coli when it was administered at one day of age by coarse spray.

EXAMPLE 9 Comparative Study A

In this study, the vaccine of the invention was compared against the commercial GARAVAX®-T vaccine, a competitor's product, which is a live bacterial vaccine containing an a virulent temperature sensitive mutant of E. coli, and is recommended for use in turkeys to aid in the prevention of colibacillosis associated with infection by E. coli serotype O78.

Each bird in test group #1 (30 birds) was vaccinated by coarse spray at 1 day of age and again in the drinking water at 2 weeks of age with one bird dose of E. coli aroA-vaccine according to one embodiment of the invention (passage level X+5; 5.0×10⁶ cfu per 1 mL dose). Birds in test group #2 (30 birds) were each vaccinated by coarse spray at 1 day of age and again in the drinking water at 2 weeks of age with one bird dose of GARAVAX®-T vaccine, following recommended label directions. Birds in test group #3 (30 birds) served as unvaccinated challenged controls. Birds in test group #4 (30 birds) were not vaccinated and were not challenged. All the birds in groups #1, #2 and #3 were challenged intratracheally at 6 weeks of age with a target dose of 5×10⁹ cfu per dose (1.0 mL/dose) of a virulent E. coli O78. At 7 days post challenge, the number of dead birds was noted and all surviving birds were necropsied and examined for the presence of grossly visible lesions typical of colibacillosis.

The results are set forth in Table III below—the percentages of chickens with specific airsacculitis and overall colibacillosis lesions is quantified therein:

TABLE III Total % Positive % Positive Group Vaccination Challenge No. for for No. Route Route Birds Airsacculitis Colibacillosis Airsacculitis¹ Colibacillosis² EFFICACY OF LIVE E. COLI AROA-VACCINE IN PREVENTING AIRSACCULITIS IN CHICKENS AGAINST E. COLI O78 CHALLENGE 1 CS/DW Intratracheally 30 2 2 6.6 (2/30^(a)) 6.6 (2/30^(a)) 3 None Intratracheally 30 16 19 53.3 (16/30^(b)) 63.3 (19/30^(b)) Efficacy of GARAVAX ®-T VACCINE in preventing airsacculitis in chickens against E. coli O78 CHALLENGE 2 CS/DW Intratracheally 30 8 10 26.7 (8/30^(a))  33.3 (10/30^(a)) 3 None Intratracheally 30 16 19 53.3 (16/30^(b)) 63.3 (19/30^(b)) ¹% Positive for airsacculitis = Total # of birds with airsacculitis/total # of birds ²% Positive for colibacillosis = Total # of birds with colibacillosis lesions and birds dead/total # of birds CS = Coarse Spray DW = Drinking Water Values within the same column followed by different letters are significantly different (Chi-square test: p < 0.05)

EXAMPLE 10 Comparative Study B

In this study, the vaccine of the invention was compared against the commercial GARAVAX®-T vaccine, a competitor's product, which is a live bacterial vaccine containing an a virulent temperature sensitive mutant of E. coli, and is recommended for use in turkeys to aid in the prevention of colibacillosis associated with infection by E. coli serotype O78.

Each bird in test group #1 (31 birds) was vaccinated by coarse spray at 1 day of age and again in the drinking water at 2 weeks of age with one bird dose of E. coli aroA-vaccine according to one embodiment of the invention (passage level X+5; 5.0×10⁶ cfu per 1 mL dose). Birds in test group #2 (29 birds) were each vaccinated by coarse spray at 1 day of age and again in the drinking water at 2 weeks of age with one bird dose of GARAVAX®-T vaccine, following recommended label directions. Birds in test group #3 (31 birds) served as unvaccinated challenged controls. Birds in test group #4 (30 birds) were not vaccinated and were not challenged; none of these died. All the birds in groups #1, #2 and #3 were challenged intratracheally at 6 weeks of age with a target dose of 5.0×10⁹ cfu per dose (1.0 mL/dose) of a virulent E. coli 624 (untyped serotype). At 7 days post challenge, the number of dead birds was noted and all surviving birds were necropsied and examined for the presence of grossly visible lesions typical of colibacillosis.

The results are set forth in Table IV below—the percentages of chickens with specific cellulitis is quantified therein:

TABLE IV Total % Positive Group Vaccination Challenge No. No. Dead for No. Route Route Birds Cellulitis Birds Cellulitis¹ EFFICACY OF LIVE E. COLI AROA-VACCINE IN PREVENTING CELLULITIS IN CHICKENS AGAINST E. COLI 624 (UNTYPED SEROTYPE) CHALLENGE 1 CS/DW Intratracheally 31 6 8 45.2 (14/31^(a)) 3 None Intratracheally 31 4 20 77.4 (24/31^(b)) EFFICACY OF GARAVAX ®-T VACCINE IN PREVENTING CELLULITIS IN CHICKENS AGAINST E. COLI 624 (UNTYPED SEROTYPE) CHALLENGE 2 CS/DW Intratracheally 29 7 12 65.5 (19/29^(a)) 3 None Intratracheally 31 4 20 77.4 (24/31^(a)) ¹% Positive for Cellulitis = Total # of birds w/cellulitis and birds dead/total # of birds CS = Coarse Spray DW = Drinking Water Values within the same column followed by different letters are significantly different (Chi-square test: p < 0.05) 

1. A method for the prevention or amelioration of at least one symptom associated with colibacillosis in poultry which comprises administering to said poultry an immunogenically effective amount of an isolated aroA mutant E. coil strain, wherein the aroA mutant E. coil strain is the strain deposited at the American Type Culture Collection under assigned number PTA-5094.
 2. The method of claim 1, wherein at least one of the symptoms is septicemia, pericarditis, airsacculitis, periphepatitis, arthritis, or cellulitis.
 3. The method of claim 2 wherein the colibacillosis symptom is septicemia.
 4. The method of claim 2 wherein the colibacillosis symptom is pericarditis.
 5. The method of claim 2 wherein the colibacillosis symptom is airsacculitis.
 6. The method of claim 2 wherein the colibacillosis symptom is periphepatitis.
 7. The method of claim 2 wherein the colibacillosis symptom is arthritis.
 8. The method of claim 2 wherein the colibacillosis symptom is cellulitis. 